Clinical Institute of the Brain, Ural Department, Russian Academy of Medical Sciences, Yasnaya str. 38, 620102, Yekaterinburg, Russia.
Transl Stroke Res. 2011 Sep;2(3):358-65. doi: 10.1007/s12975-011-0091-3. Epub 2011 Aug 4.
Granulocyte-colony-stimulating factor (G-CSF) functions both as a neuroprotectant and a stimulator of autologous bone marrow stem cell release. Therefore, administration of G-CSF should improve the outcome of stroke. Here, we examine the safety of using G-CSF to treat acute ischemic stroke using a randomized controlled trial involving 20 adult patients presenting with ischemia in the carotid region within 48 h of onset. The experimental group (n = 10) received subcutaneous G-CSF injections (10 mg kg(-1) day(-1)) in addition to conventional therapy for 5 days. The primary outcome was motor function as measured by the modified Rankin Scale 180 days post-stroke. Safety was evaluated according to the frequency of hemorrhagic transformation of infarctions and serious adverse events. Only six patients in the experimental group completed full course of treatment, while four patients (three in the control and one in the experimental group) were lost to follow-up. We found the experimental and control groups did not differ significantly in either neurological impairment or degree of disability/dependence at 180 days post-stroke. We conclude that while adding G-CSF (10 mg kg(-1) day(-1)) to acute ischemic stroke therapy for 5 days is safe, its efficacy remains unproven.
粒细胞集落刺激因子(G-CSF)兼具神经保护和刺激自体骨髓干细胞释放的作用。因此,G-CSF 的给药应该可以改善中风的预后。在这里,我们通过一项涉及 20 名成年患者的随机对照试验来检查使用 G-CSF 治疗颈动脉区域急性缺血性中风的安全性,这些患者在发病后 48 小时内出现缺血。实验组(n = 10)除了接受常规治疗外,还额外接受 5 天的皮下 G-CSF 注射(10 mg·kg-1·d-1)。主要结局是中风后 180 天通过改良 Rankin 量表评估的运动功能。安全性根据梗死出血转化的频率和严重不良事件来评估。实验组只有 6 名患者完成了全程治疗,而对照组有 4 名患者(3 名)和实验组有 1 名患者失访。我们发现实验组和对照组在中风后 180 天的神经功能损伤或残疾/依赖程度方面没有显著差异。我们得出结论,在急性缺血性中风治疗中添加 5 天 10 mg·kg-1·d-1 的 G-CSF 是安全的,但疗效仍未得到证实。